A randomized comparison of radial artery injury after 6.0-Fr glide sheath and 6.5-Fr sheathless transradial coronary intervention using FD-OCT/OFDI.
Not Applicable
- Conditions
- Consecutive patients with ischemic heart disease who underwent elective transradial coronary intervention using FD-OCT/OFDI.
- Registration Number
- JPRN-UMIN000029037
- Lead Sponsor
- Japan Community Healthcare Organization Tokuyama Central Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with serum creatinine > 2.0mg/dl or abnormal Allen test.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is to assess the radial artery injury (intimal flap, medial dissection or thrombus) using FD-OCT/OFDI.
- Secondary Outcome Measures
Name Time Method The secondary endpoints include radial artery spasm, procedure time ,amount of contrast media and ultrasound-evaluated radial artery occlusion at 8-12 months.